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Catalog Number:
40153
CAS Number:
204841-19-0
3-Acetylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Acetylbenzeneboronic acid
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Product Information

3-Acetylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a phenyl ring with an acetyl group, enhancing its reactivity and making it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique ability to form reversible covalent bonds with diols makes it particularly valuable in the synthesis of complex molecules, including glycosylation reactions and the development of boron-based sensors. Researchers appreciate its role in cross-coupling reactions, which are pivotal in creating diverse organic compounds.

In addition to its synthetic applications, 3-Acetylphenylboronic acid has shown promise in the field of cancer research, where it is being explored for its potential to inhibit specific enzymes involved in tumor growth. Its favorable solubility and stability under various conditions further enhance its applicability in both laboratory and industrial settings. With its multifunctional properties, this compound stands out as a crucial reagent for professionals seeking to innovate in chemical synthesis and drug development.

Synonyms
3-Acetylbenzeneboronic acid
CAS Number
204841-19-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H9BO3
Molecular Weight
163.97
MDL Number
MFCD01074678
PubChem ID
2734310
Melting Point
208 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Acetylbenzeneboronic acid
CAS Number
204841-19-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H9BO3
Molecular Weight
163.97
MDL Number
MFCD01074678
PubChem ID
2734310
Melting Point
208 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Acetylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It plays a crucial role in drug discovery, especially in the design of inhibitors for certain enzymes, which can lead to new treatments for diseases.
  • Materials Science: The compound is used in the preparation of functional materials, such as polymers and nanomaterials, which have applications in electronics and coatings.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces, enhancing the performance of biosensors and diagnostic tools.
  • Cross-Coupling Reactions: This chemical is integral in cross-coupling reactions, a fundamental process in organic chemistry that allows for the formation of carbon-carbon bonds, essential for creating complex molecules.

Citations